Works by Lars Allan Larsen

Results: 27

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.

Published in:

Human Mutation, 2009, v. 30, n. 3, p. 363, doi. 10.1002/humu.20862

By:

Andersen, Paal Skytt;
Havndrup, Ole;
Hougs, Lotte;
Sørensen, Karina M.;
Jensen, Morten;
Larsen, Lars Allan;
Hedley, Paula;
Bie Thomsen, Alex Rojas;
Moolman-Smook, Johanna;
Christiansen, Michael;
Bundgaard, Henning

Publication type:

Article

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening (Communicated by Mireille Claustres).

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 455, doi. 10.1002/humu.10169

By:

Paal Skytt Andersen;
Cathrine Jespersgaard;
Jens Vuust;
Michael Christiansen;
Lars Allan Larsen

Publication type:

Article

Capillary electrophoresis‐based single strand DNA conformation analysis in high‐throughput mutation screeningCommunicated by Mireille Claustres.

Published in:

Human Mutation, 2003, v. 21, n. 5, p. 455, doi. 10.1002/humu.10169

By:

Paal Skytt Andersen;
Cathrine Jespersgaard;
Jens Vuust;
Michael Christiansen;
Lars Allan Larsen

Publication type:

Article

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method.

Published in:

Human Mutation, 2003, v. 21, n. 2, p. 116, doi. 10.1002/humu.10161

By:

Andersen, Paal Skytt;
Jespersgaard, Cathrine;
Vuust, Jens;
Christiansen, Michael;
Larsen, Lars Allan

Publication type:

Article

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis.

Published in:

Human Mutation, 2001, v. 18, n. 5, p. 451, doi. 10.1002/humu.1216

By:

Larsen, Lars Allan;
Johnson, Martin;
Brown, Candia;
Christiansen, Michael;
Frank-Hansen, Rune;
Vuust, Jens;
Andersen, Paal Skytt

Publication type:

Article

MCPH1: A Novel Case Report and a Review of the Literature.

Published in:

Genes, 2022, v. 13, n. 4, p. 634, doi. 10.3390/genes13040634

By:

Caraffi, Stefano Giuseppe;
Pollazzon, Marzia;
Farooq, Muhammad;
Fatima, Ambrin;
Larsen, Lars Allan;
Zuntini, Roberta;
Napoli, Manuela;
Garavelli, Livia

Publication type:

Article

Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 8, p. 1010, doi. 10.1038/ejhg.2008.269

By:

Zhang, Litu;
Tümer, Zeynep;
Møllgård, Kjeld;
Barbi, Gotthold;
Rossier, Eva;
Bendsen, Eske;
Møller, Rikke Steensbjerre;
Ullmann, Reinhard;
Jian He;
Papadopoulos, Nickolas;
Tommerup, Niels;
Larsen, Lars Allan

Publication type:

Article

One-third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region.

Published in:

2005

By:

Hougs, Lotte;
Havndrup, Ole;
Bundgaard, Henning;
Køber, Lars;
Vuust, Jens;
Larsen, Lars Allan;
Christiansen, Michael;
Andersen, Paal Skytt

Publication type:

Correction Notice

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 2, p. 161, doi. 10.1038/sj.ejhg.5201310

By:

Hougs, Lotte;
Havndrup, Ole;
Bundgaard, Henning;
Køber, Lars;
Vuust, Jens;
Larsen, Lars Allan;
Christiansen, Michael;
Andersen, Paal Skytt

Publication type:

Article

Analysis of FMR1 (CGG)<sub>n</sub> alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 9, p. 724, doi. 10.1038/sj.ejhg.5200697

By:

Larsen, Lars Allan;
Vuust, Jens;
Nystad, Mona;
Evseeva, Irina;
Van Ghelue, Marijke;
Tranebjærg, Lisbeth

Publication type:

Article

Analysis of FMR1 (CGG)<sub>n</sub> alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 7, p. 771, doi. 10.1038/sj.ejhg.5200374

By:

Larsen, Lars Allan;
Armstrong, Judith SM;
Grønskov, Karen;
Hjalgrim, Helle;
Brøndum-Nielsen, Karen;
Hasholt, Lis;
Nørgaard-Pedersen, Bent;
Vuust, Jens

Publication type:

Article

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 6, p. 724, doi. 10.1038/sj.ejhg.5200323

By:

Larsen, Lars Allan;
Fosdal, Inger;
Andersen, Paal Skytt;
Kanters, Jørgen K;
Vuust, Jens;
Wettrell, Göran;
Christiansen, Michael

Publication type:

Article

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac β-myosin gene mutations

Published in:

Cardiovascular Research, 2003, v. 57, n. 2, p. 347, doi. 10.1016/S0008-6363(02)00711-3

By:

Havndrup, Ole;
Bundgaard, Henning;
Skytt Andersen, Paal;
Allan Larsen, Lars;
Vuust, Jens;
Kjeldsen, Keld;
Christiansen, Michael

Publication type:

Article

Pericardial delta like non‐canonical NOTCH ligand 1 (Dlk1) augments fibrosis in the heart through epithelial to mesenchymal transition.

Published in:

Clinical & Translational Medicine, 2024, v. 14, n. 2, p. 1, doi. 10.1002/ctm2.1565

By:

Jensen, Charlotte Harken;
Johnsen, Rikke Helin;
Eskildsen, Tilde;
Baun, Christina;
Ellman, Ditte Gry;
Fang, Shu;
Bak, Sara Thornby;
Hvidsten, Svend;
Larsen, Lars Allan;
Rosager, Ann Mari;
Riber, Lars Peter;
Schneider, Mikael;
De Mey, Jo;
Thomassen, Mads;
Burton, Mark;
Uchida, Shizuka;
Laborda, Jorge;
Andersen, Ditte Caroline

Publication type:

Article

Screening of congenital heart disease patients using multiplex ligation-dependent probe amplification: Early diagnosis of syndromic patients.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 720, doi. 10.1002/ajmg.a.35214

By:

Sørensen, Karina Meden;
El-Segaier, Milad;
Fernlund, Eva;
Errami, Ab;
Bouvagnet, Patrice;
Nehme, Nancy;
Steensberg, Jesper;
Hjortdal, Vibeke;
Soller, Maria;
Behjati, Mohaddeseh;
Werge, Thomas;
Kirchoff, Maria;
Schouten, Jan;
Tommerup, Niels;
Andersen, Paal Skytt;
Larsen, Lars Allan

Publication type:

Article

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy.

Published in:

2000

By:

Havndrup, Ole;
Bundgaard, Henning;
Andersen, Paal Skytt;
Larsen, Lars Allan;
Vuust, Jens;
Kjeldsen, Keld;
Christiansen, Michael;
Havndrup, O;
Bundgaard, H;
Andersen, P S;
Larsen, L A;
Vuust, J;
Kjeldsen, K;
Christiansen, M

Publication type:

journal article

222: FAMILIAL RECURRENCE OF CONGENITAL HEART DISEASE CAUSED BY MUTATION IN NKX2-5.

Published in:

Cardiovascular Journal of Africa, 2013, v. 24, n. 1, p. 148

By:

Eliasson, Sabrina;
Hjortdal, Vibeke;
Bjerre, Jesper;
Søndergaard, Lars;
Andersen, Henrik Ãrbãk;
Brunak, Søren;
Jensen, Anders Boeck;
Larsen, Lars Allan

Publication type:

Article

Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics.

Published in:

Electrophoresis, 2006, v. 27, n. 19, p. 3816

By:

Cathrine Jespersgaard;
Lars Allan Larsen;
Shingo Baba;
Yoji Kukita;
Tomoko Tahira;
Michael Christiansen;
Jens Vuust;
Kenshi Hayashi;
Paal Skytt Andersen

Publication type:

Article

High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device.

Published in:

Electrophoresis, 2005, v. 26, n. 9, p. 1834, doi. 10.1002/elps.200410205

By:

Huijun Tian;
Charles A. Emrich;
James R. Scherer;
Richard A. Mathies;
Paal Skytt Andersen;
Lars Allan Larsen;
Michael Christiansen

Publication type:

Article

IFT20 modulates ciliary PDG FRα signaling by regulating the stability of Cbl E3 ubiquitin ligases.

Published in:

Journal of Cell Biology, 2018, v. 217, n. 1, p. 151, doi. 10.1083/jcb.201611050

By:

Schmid, Fabian Marc;
Schou, Kenneth Bødtker;
Vilhelm, Martin Juel;
Holm, Maria Schrøder;
Breslin, Loretta;
Farinelli, Pietro;
Larsen, Lars Allan;
Andersen, Jens Skorstengaard;
Pedersen, Lotte Bang;
Christensen, Søren Tvorup

Publication type:

Article

GLI1 Is Involved in Cell Cycle Regulation and Proliferation of NT2 Embryonal Carcinoma Stem Cells.

Published in:

DNA & Cell Biology, 2008, v. 27, n. 5, p. 251, doi. 10.1089/dna.2007.0625

By:

Vestergaard, Janni;
Lind-Thomsen, Allan;
Pedersen, Mikkel W.;
Jarmer, Hanne Østergaard;
Bak, Mads;
Hasholt, Lis;
Tommerup, Niels;
Tümer, Zeynep;
Larsen, Lars Allan

Publication type:

Article

Novel Donor Splice Site Mutation in the KVLQT1 Gene is Associated with Long QT Syndrome.

Published in:

Journal of Cardiovascular Electrophysiology, 1998, v. 9, n. 6, p. 620, doi. 10.1111/j.1540-8167.1998.tb00944.x

By:

Kanters, J&oslashrgen K.;
Allan Larsen, Lars;
Orholm, Marianne;
Agner, Erik;
Andersen, Paal Skytt;
Vuust, Jens;
Christiansen, Michael

Publication type:

Article

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.

Published in:

Clinical Genetics, 2000, v. 57, n. 2, p. 125, doi. 10.1034/j.1399-0004.2000.570206.x

By:

Allan Larsen, Lars;
Hastrup Svendsen, Ida;
Møller Jensen, Annette;
Kanters, Jørgen K;
Skytt Andersen, Paal;
Møller, Mogens;
Asger Sørensen, Sven;
Sandøe, Erik;
Ramsøe Jacobsen, Joes;
Vuust, Jens;
Christiansen, Michael

Publication type:

Article

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants.

Published in:

Human Mutation, 1999, v. 13, n. 4, p. 318, doi. 10.1002/(SICI)1098-1004(1999)13:4<318::AID-HUMU9>3.0.CO;2-F

By:

Larsen, Lars Allan;
Christiansen, Michael;
Vuust, Jens;
Andersen, Paal Skytt

Publication type:

Article

Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients.

Published in:

Human Genetics, 2024, v. 143, n. 11, p. 1323, doi. 10.1007/s00439-024-02703-z

By:

Baird, Daniel A.;
Mubeen, Hira;
Doganli, Canan;
Miltenburg, Jasmijn B.;
Thomsen, Oskar Kaaber;
Ali, Zafar;
Naveed, Tahir;
Rehman, Asif ur;
Baig, Shahid Mahmood;
Christensen, Søren Tvorup;
Farooq, Muhammad;
Larsen, Lars Allan

Publication type:

Article

Cilia and coordination of signaling networks during heart development.

Published in:

Organogenesis, 2014, v. 10, n. 1, p. 1, doi. 10.4161/org.27483

By:

Koefoed, Karen;
Veland, Iben Rønn;
Pedersen, Lotte Bang;
Larsen, Lars Allan;
Christensen, Søren Tvorup

Publication type:

Article

Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.

Published in:

Congenital Heart Disease, 2016, v. 11, n. 3, p. 283, doi. 10.1111/chd.12317

By:

Ellesøe, Sabrina Gade;
Johansen, Morten Munk;
Bjerre, Jesper Vandborg;
Hjortdal, Vibeke Elisabeth;
Brunak, Søren;
Larsen, Lars Allan

Publication type:

Article